HIV/AIDS Research: AIDS-related virus tricks cells to become tumors

AIDSWEEKLY Plus; Monday, November 27, 2006
Staff Medical Writers

KSHV is an opportunistic pathogen that rarely affects individuals with normal immune systems. However, HIV/AIDS patients and those who are immune suppressed such as organ transplant patients are at high risk for developing Kaposi's sarcoma and another cancer called primary effusion lymphoma.

The study describes how a KSHV-encoded protein, called latency-associated nuclear antigen, or LANA, tricks the cell into destroying two major suppressors of tumor growth called von Hippel Lindau (VHL) and p53. "In addition, we have shown that when LANA expression was blocked, the tumor suppressors again become stable suggesting a direct role of the viral protein in regulation of these major cell proteins," said lead author Erle Robertson, PhD, Professor of Microbiology and the Director of Tumor Virology at Penn's Abramson Cancer Center.

The trick is played out in a cell process called ubiquitylation. This refers to a pathway in all cells whereby a protein aptly named ubiquitin binds to cellular proteins and marks them for degradation. This process can be likened to putting out the garbage for disposal.

Ubiquitylation and degradation involve a complex set of proteins in addition to ubiquitin. "We found that the viral LANA has an amino acid motif that mimics non-viral cell proteins usually involved in the ubiquitylation process," said Robertson. This motif, or stretch of amino acids, normally enables LANA to bind to tumor suppressors p53 or VHL, thus bringing them into the active ubiquitylation complex. Once in the complex, the tumor suppressors are targeted for degradation.

Tumor suppressors, as their name implies, prevent or limit the growth of tumors in numerous ways. One way the tumor suppressors p53 and VHL work is to mark a key protein that controls the blood supply in a tumor mass. Once marked, this protein called hypoxia-induced factor 1a (HIF-1a) is degraded through ubiquitylation before it can start the process of activating genes responsible for inducing growth of more blood vessels to supply the tumor with oxygen. However, in a KSHV-infected cell, p53 and VHL themselves would be targeted for degradation and HIF-1a would then be free to activate genes involved in growth of blood vessels to increase the blood supply to the tumor.

"Use of such proteosome inhibitors as Bortezomib as cancer therapeutic agents has been ongoing for the last four to five years and this study provides crucial step in understanding the mechanism for anti-tumorigenic activity against KSHV-associated human cancers," concludes Robertson. "Additionally, we can now use compounds known to inhibit proteosome activity to determine their effectiveness in inhibiting the Kaposi's viral-induced degradation of these two major tumor suppressors." This, he said, is important in finding or designing drugs that can be specifically used against KSHV, and potentially, other virus-associated cancers.

This article was prepared by AIDS Weekly editors from staff and other reports.

2006-11-27
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